Stereoselective synthesis of the macrocyclic core of salicylihalamides A and B is described. The synthetic strategy features stereoselective iodolactonization, Sharpless asymmetric epoxidation, Mitsunobu esterification, and ring-closing metathesis
Access restricted to the OSU CommunityA flexible, convergent-divergent strategy for the asymmetric t...
Concise, flexible and high yielding approaches to the orsellinic acid type macrolides lasiodiplodin ...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our...
Beim Aufspüren biologisch aktiver Substanzen erlangen zunehmend auch marine Organismen und deren Sto...
An efficient synthesis of the macrolactone 3 of the salicylihalamides in 10 linear steps from alkene...
A catalysis-based approach to the core region 24 of the antitumor agents salicylihalamides A and B i...
A concise total synthesis of the potent cytotoxic marine natural products salicylihalamide A and B (...
Formal total synthesis of (−)-salicylihalamides A and B is described starting with a nonracemic chir...
In den letzen Jahren wurde von verschiedenen Arbeitsgruppen über Naturstoffe berichtet, die alle zu ...
A concise formal synthesis of the cytotoxic macrolides (-)-salicylihalamides A and B is reported. Ke...
<p>A simple and efficient stereoselective total synthesis of sporiolide B and attempted synthesis of...
The first part of this dissertation describes the total synthesis of (+)- and (−)-salicylihalamide A...
This thesis describes studies toward the synthesis of enamide macrolide salicylihalamide A (1). The...
The diastereoselective synthesis of the macrolactone core of amphidinolide W was successfully accomp...
Access restricted to the OSU CommunityA flexible, convergent-divergent strategy for the asymmetric t...
Concise, flexible and high yielding approaches to the orsellinic acid type macrolides lasiodiplodin ...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
A stereoselective and convergent formal approach to Salicylihalamide A and B is achieved through our...
Beim Aufspüren biologisch aktiver Substanzen erlangen zunehmend auch marine Organismen und deren Sto...
An efficient synthesis of the macrolactone 3 of the salicylihalamides in 10 linear steps from alkene...
A catalysis-based approach to the core region 24 of the antitumor agents salicylihalamides A and B i...
A concise total synthesis of the potent cytotoxic marine natural products salicylihalamide A and B (...
Formal total synthesis of (−)-salicylihalamides A and B is described starting with a nonracemic chir...
In den letzen Jahren wurde von verschiedenen Arbeitsgruppen über Naturstoffe berichtet, die alle zu ...
A concise formal synthesis of the cytotoxic macrolides (-)-salicylihalamides A and B is reported. Ke...
<p>A simple and efficient stereoselective total synthesis of sporiolide B and attempted synthesis of...
The first part of this dissertation describes the total synthesis of (+)- and (−)-salicylihalamide A...
This thesis describes studies toward the synthesis of enamide macrolide salicylihalamide A (1). The...
The diastereoselective synthesis of the macrolactone core of amphidinolide W was successfully accomp...
Access restricted to the OSU CommunityA flexible, convergent-divergent strategy for the asymmetric t...
Concise, flexible and high yielding approaches to the orsellinic acid type macrolides lasiodiplodin ...
A total, stereoselective synthesis of the cytotoxic macrolide aspergillide B has been performed. A c...
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